510(k) K832446 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered
CATAREX DIAP. EXTRACAPSULAR CATARACT
| Applicant | Calliope Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 19, 1983 |
| Received | Jul 25, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832446
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.